Canonical Allele Identifier: CA2620331694
Gene: TMPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.98534338_98534339del , CM000674.2:g.98534338_98534339del GRCh38
NC_000012.11:g.98928116_98928117del , CM000674.1:g.98928116_98928117del GRCh37
NC_000012.10:g.97452247_97452248del NCBI36
NG_021393.1:g.23766_23767del , LRG_443:g.23766_23767del

Transcript Alleles

HGVS Amino-acid change
ENST00000556029.6:c.565+2500_565+2501del MANE Select ENSP00000450627.1:n.565+2500_565+2501del
ENST00000261210.9:c.565+2500_565+2501del ENSP00000261210.5:n.565+2500_565+2501del
ENST00000266732.8:c.2081_2082del ENSP00000266732.4:p.His694LeufsTer25
ENST00000343315.9:c.565+2500_565+2501del ENSP00000340251.5:n.565+2500_565+2501del
ENST00000393053.6:c.565+2500_565+2501del ENSP00000376773.2:n.565+2500_565+2501del
ENST00000552831.1:n.643+2500_643+2501del
ENST00000556029.5:c.565+2500_565+2501del ENSP00000450627.1:n.565+2500_565+2501del
ENST00000556678.1:c.286+2500_286+2501del ENSP00000451552.1:n.286+2500_286+2501del
NM_001032283.2:c.565+2500_565+2501del , LRG_443t1:c.565+2500_565+2501del NP_001027454.1:n.565+2500_565+2501del
NM_001032284.2:c.565+2500_565+2501del NP_001027455.1:n.565+2500_565+2501del
NM_001307975.1:c.565+2500_565+2501del NP_001294904.1:n.565+2500_565+2501del
NM_003276.2:c.2081_2082del , LRG_443t2:c.2081_2082del NP_003267.1:p.His694LeufsTer25
XM_005269132.2:c.565+2500_565+2501del XP_005269189.1:n.565+2500_565+2501del
XM_005269132.4:c.565+2500_565+2501del XP_005269189.1:n.565+2500_565+2501del
XM_017019914.2:c.1175_1176del XP_016875403.1:p.His392LeufsTer25
NM_001032283.3:c.565+2500_565+2501del MANE Select NP_001027454.1:n.565+2500_565+2501del
NM_001032284.3:c.565+2500_565+2501del NP_001027455.1:n.565+2500_565+2501del
NM_001307975.2:c.565+2500_565+2501del NP_001294904.1:n.565+2500_565+2501del